首页> 外文期刊>International Journal of Quantum Chemistry >On the definition of the atomic charge. Relationship between C-13 NMR chemical shifts, dipole moments, and charges in saturated hydrocarbons
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On the definition of the atomic charge. Relationship between C-13 NMR chemical shifts, dipole moments, and charges in saturated hydrocarbons

机译:关于原子电荷的定义。 C-13 NMR化学位移,偶极矩与饱和烃中电荷之间的关系

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The problem of defining a reliable quantum mechanical charge by comparison with one-electron properties is analyzed, and it is stressed that properties involving the virtual space are not suited to that end. Particular attention is devoted to the relationship between charges and chemical shifts for the case of saturated hydrocarbons. A simple explanation of the Grant and Paul alpha effect is suggested, which can also account for the modified population analysis proposed by Fliszar. Moreover the vexata quaestio of the direction of the C-H bond dipole moment has been reexamined. The awkward theoretical prediction (C+-H-) can be reconciled with the one based on experimental data and electronegativities (C--H+) if one considers that the former is determined by an hydridization contribution to the dipole moment, which tend to cancel in a summation over all the bonds formed by each atom. (C) 1998 John Wiley & Sons, Inc. [References: 40]
机译:分析了通过与单电子性质比较来定义可靠的量子力学电荷的问题,并强调了涉及虚拟空间的性质不适合该目的。对于饱和烃,特别要注意电荷与化学位移之间的关系。建议对Grant和Paul alpha效应进行简单的解释,这也可以解释Fliszar提出的修改后的人口分析。此外,已经重新检查了C-H键偶极矩方向的正点状准点。如果有人认为前者是由对偶极矩的加氢作用决定的,则笨拙的理论预测(C + -H-)可与基于实验数据和电负性(CH--H +)的理论预测相吻合,后者在每个原子形成的所有键的总和。 (C)1998 John Wiley&Sons,Inc. [参考:40]

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